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FDA 510(k) Applications Submitted by Synergy Biomedical, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K173301
10/17/2017
BioSphere MIS Putty (BioSphere MIS)
Synergy Biomedical, Llc
K122868
09/18/2012
BIOSPHERE BIOACTIVE BONE GRAFT PUTTY
Synergy Biomedical, LLC
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